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IDPH is first step in Zika testing

Photo of mosquito
Feb. 4, 2016 -- Healthcare providers suspecting a potential case of Zika virus should first contact the Iowa Department of Public Health’s Center for Acute Disease Epidemiology at 800-362-2736. CADE staff will consult with the provider to determine whether the case meets the CDC testing criteria.

Zika virus testing should be considered for patients with acute fever, rash, myalgia, or arthralgia who have traveled within the previous two weeks to an area with ongoing transmission of those viruses or are living in an area with ongoing transmission.

During the first week after onset of symptoms, Zika virus disease can often be diagnosed by performing reverse transcriptase-polymerase chain reaction (RT-PCR) on serum. Virus-specific IgM and neutralizing antibodies typically develop toward the end of the first week of illness; cross-reaction with related flaviviruses (e.g., dengue and yellow fever viruses) is common and may be difficult to discern. Plaque-reduction neutralization testing can be performed to measure virus-specific neutralizing antibodies and discriminate between cross-reacting antibodies in primary flavivirus infections.

CDC recommends serologic testing for asymptomatic pregnant women with a history of travel (2 to 12 weeks post travel) to areas with local transmission of Zika virus or who are living in an area with ongoing transmission.

The most recent information concerning affected countries, symptoms, treatment, etc. can be found on the CDC Zika web page.

Image of Zika virus / pregnancy info-graphic.
The following information is for Iowa clinical and hospital laboratories.

Diagnostic Testing:

The specific tests performed will depend on the timing of the specimens relative to illness onset and clinical information as outlined in the testing algorithm.

Please provide the date of illness onset, dates of specimen collection, specimen type, description of clinical illness, travel history, flavivirus vaccination history, and contact information for the submitter. Testing primarily will be performed on serum or CSF.

Zika Virus Specimen Collection and Submission Instructions:

Adults

Serum- at least 1.0 mL send cold on ice packs or frozen.

IF CSF is already collected and available, send 0.5mL frozen.

Infants

Serum-at least 1.0 mL, send cold on ice packs or frozen.

Amniotic fluid or cord blood -at least 1.0 mL, send frozen.

Placenta- portion in sterile container, send frozen.

Note: Samples that are to be sent frozen should be frozen as immediately as possible after collection.

Laboratory safety:

Zika virus is classified as a biological safety level (BSL) 2 pathogen. It should be handled in accordance with Biosafety in Microbiological and Biomedical Laboratories (BMBL) guidelines and a laboratory risk assessment should be performed for the specific procedures utilized for testing specimens from patients suspected of carrying the virus.

Results:

Test turn-around time is expected to be within 7 days. There may be delays if confirmatory testing is required.

ALL RESULTS WILL BE SENT TO THE APPROPRIATE STATE OR LOCAL HEALTH DEPARTMENT.

Reporting:

Zika, dengue and chikungunya are all nationally notifiable conditions. Health care providers are encouraged to report suspected cases to their state or local health department to facilitate diagnosis and mitigate the risk of local transmission.

Resources:

The toll-free number for these contacts is 800-421-IOWA (4692).